ChemicalBook > Product Catalog >Pharmaceutical intermediates >Heterocyclic compound >Pyridazine compounds >3,4,6-Trichloropyridazine

3,4,6-Trichloropyridazine

3,4,6-Trichloropyridazine Suppliers list
Company Name: Nanbu County Chengxin Technology Co., Ltd.  Gold
Tel: 0838-5675166 15883665058
Email: nbcxkj@126.com
Company Name: Beijing Taiya Jie Technology Development Co., Ltd.  Gold
Tel: 021-33690831-8001 13552411790;18616022633
Email: postmaster@tyjchem.cn
Company Name: Tianmen Hengchang Chemical Co., Ltd  Gold
Tel: 027-59322316 15172518801
Email: 1208480077@qq.com
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
Email: market03@meryer.com

3,4,6-Trichloropyridazine manufacturers

3,4,6-Trichloropyridazine Basic information
Product Name:3,4,6-Trichloropyridazine
Synonyms:3,4,6-Trichloro-1,2-diazine;3,4,6-TRICHLOROPYRIDAZINE;3-METHYL-2-BENZOXAZOLINONE,PLANT STANDARD;3,4,6-TrichL;6-Trichloropyridazine;Pyridazine, 3,4,6-trichloro-;3,4,6-Trichloropyridazine ISO 9001:2015 REACH
CAS:6082-66-2
MF:C4HCl3N2
MW:183.42
EINECS:629-902-8
Product Categories:alkyl chloride
Mol File:6082-66-2.mol
3,4,6-Trichloropyridazine Structure
3,4,6-Trichloropyridazine Chemical Properties
Melting point 55.0 to 59.0 °C
Boiling point 98°C/43mmHg(lit.)
density 1.641±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility soluble in Methanol
form powder to crystal
pka-2.72±0.10(Predicted)
color White to Light yellow to Light orange
λmax305nm(EtOH)(lit.)
InChIInChI=1S/C4HCl3N2/c5-2-1-3(6)8-9-4(2)7/h1H
InChIKeyLJDQXQOPXOLCHL-UHFFFAOYSA-N
SMILESC1(Cl)=NN=C(Cl)C=C1Cl
Safety Information
HazardClass IRRITANT
HS Code 2933998090
MSDS Information
3,4,6-Trichloropyridazine Usage And Synthesis
Uses3,4,6-Trichloropyridazine was used to study chloropyridazine derivatives as human rhinovirus capsid-binding inhibitors.
Materials Uses3,4,6-Trichloropyridazine is a kind of new liquid crystal industrial raw material.
Synthesis
3,6-Dichloropyridazine

141-30-0

3,4,6-Trichloropyridazine

6082-66-2

The general procedure for the synthesis of 3,4,6-trichloropyridazine from 3,6-dichloropyridazine is as follows: 44 g of 3,6-dichloropyridazine and 22 g of aluminum trichloride were mixed and heated to 140°C. The mixture was then heated to 140°C for 4 hours. At this temperature, 10.6 liters of chlorine gas were slowly passed over a period of 4 hours. Upon completion of the reaction, the reaction mixture was cooled and extracted with toluene. The extract was subsequently washed with 10% sodium chloride solution and finally the product was purified by distillation to collect a fraction with a boiling point of 127-129 °C. Finally 44.1 g of 3,4,6-trichloropyridazine was obtained.

References[1] Patent: EP1900735, 2008, A1. Location in patent: Page/Page column 9
[2] Patent: US2010/305102, 2010, A1. Location in patent: Page/Page column 17
[3] Patent: US2012/28932, 2012, A1
[4] Patent: US2013/237527, 2013, A1. Location in patent: Paragraph 0236; 0237
Tag:3,4,6-Trichloropyridazine(6082-66-2) Related Product Information
Trichloroethylene Trichlormethiazide Trichloroisocyanuric acid Sucralose Trichloroacetic acid Sulfachloropyridazine sodium Hydralazine Trichlorosilane Thioridazine Chloroform 3,4,5-Trichloropyridazine 3-Methyl-2-benzoxazolinone 2-Benzoxazolinone 3,6-Dichloropyridazine 3,5-Dichloropyridazine 4-Chloropyridazine 3,4,5,6-Tetrachloropyridazine 3,4,6-Trichloropyridazine